Asthma quality of life during 1 year of treatment with budesonide with or without formoterol

被引:108
作者
Juniper, EF
Svensson, K
O'Byrne, PM
Barnes, PJ
Bauer, CA
Löfdahl, CGA
Postma, DS
Pauwels, RA
Tattersfield, AE
Ullman, A
机构
[1] McMaster Univ, Med Ctr, Dept Clin Epidemiol & Biostat, Hamilton, ON L8N 3Z5, Canada
[2] Astro Draco AB, Lund, Sweden
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] Natl Heart & Lung Inst, London, England
[5] Lurid Univ Hosp, Dept Resp Med, Lund, Sweden
[6] Univ Groningen Hosp, Dept Pulmonol, Groningen, Netherlands
[7] Univ Hosp Ghent, Dept Resp Dis, Ghent, Belgium
[8] City Hosp Nottingham, Resp Med Unit, Nottingham, England
关键词
asthma; budesonide; formoterol; quality of life;
D O I
10.1183/09031936.99.14510389
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The Formoterol and Corticosteroids Establishing Therapy (FACET) study has provided the first opportunity to examine the long-term effects of inhaled steroids and long-acting beta(2)-agonists on asthma-specific quality of life. The objectives of the present study were to: evaluate the effects of long-term (1 yr) formoterol and increasing doses of budesonide on asthma quality of life; 2) to determine whether initial improvements in quality of life are sustained when improvements in clinical indices persist; and 3) to evaluate the long-term relationship between changes in clinical indices and changes in quality of life. Of the 852 asthmatic adults enrolled, 470 from five countries participated in this quality of life evaluation. After a 4-week run-in on 1,600 mu g budesonide, patients mere randomized to either 200 mu g (Bud200) or 800 mu g budesonide (Bud800) in combination with either 24 mu g formoterol (F) or placebo daily for 1 yr. The Asthma Quality of Life Questionnaire (AQLQ) was completed and conventional clinical indices measured at enrolment and randomization and on seven occasions during the following 12 months. During the run-in, there was an improvement in AQLQ score (changes (Delta) in overall score approximate to 0.50; p<0.0001). After randomization, there was a further improvement in the Bud800+F group (Delta=0.21; p=0.028). One month post-randomization, improvements in all groups stabilized and were sustained throughout the 12 months in a pattern very similar to that observed for the conventional clinical indices. The correlation of individual patient changes in clinical indices and changes in AQLQ score during the 12-month randomized period were weak to moderate (maximum r=0.51). Improvements in quality of life, which were greatest in the 800 mu g budesonide plus 24 mu g formoterol group, were sustained throughout the 12 months in a similar manner to the clinical indices. Long-term changes in conventional clinical indices cannot be used to predict the effect of treatment on individual patient experience.
引用
收藏
页码:1038 / 1043
页数:6
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